Budesonide Inhalation Suspension
Product Images NDC 0115-1687
Product Visual Gallery
This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Budesonide Inhalation (NDC 0115-1687). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Amneal Pharmaceuticals Of New York Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
Figure 1: A 12-week Trial In Pediatric Patients Previously Maintained On Inhaled Corticosteroid Therapy Prior To Study Entry. Nighttime Asthma Change From Baseline (Budesonide Inhalation Suspension 2)
Figure 2: A 12-week Trial In Pediatric Patients Either Maintained On Bronchodilators Alone Or Inhaled Corticosteroid Therapy Prior To Study Entry. Nighttime Asthma Change From Baseline (Budesonide Inhalation Suspension 3)
Figure 1 Open The Sealed Foil Envelope Along The Dotted Line And Take Out 1 Single-dose Ampule From The Strip. (Budesonide Inhalation Suspension 4)
Figure 2 Gently Shake The Budesonide Inhalation Suspension Ampule Using A Circular Motion (Budesonide Inhalation Suspension 5)
Figure 3 Hold The Budesonide Inhalation Suspension Ampule Upright Without Squeezing The Ampule And Open By Twisting Off The Top. (Budesonide Inhalation Suspension 6)
4. Place The Open End Of The Budesonide Inhalation Suspension Ampule Into The Nebulizer Cup (reservoir) And Slowly Squeeze All Of The Medicine From The Ampule Into The Nebulizer Medicine Cup As Shown In Figure 4. Throw Away The Empty Ampule. (Budesonide Inhalation Suspension 7)
0.25 mg/2 mL Budesonide (Budesonide Inhalation Suspension 8)
0.5 mg/2ml Budesonide (Budesonide Inhalation Suspension 9)
* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.